Nature Reviews Cancer, ISSN 1474-175X, 09/2018, Volume 18, Issue 9, pp. 562 - 575
In this Opinion article, we aim to address how cells adapt to stress and the repercussions chronic stress has on cellular function. We consider acute and...
HSP90 INHIBITORS | ONCOLOGY | MOLECULAR CHAPERONES | PLANT-SPECIFIC THIOREDOXIN | POSTTRANSLATIONAL MODIFICATIONS | CONFORMATIONAL DYNAMICS | ANTITUMOR-ACTIVITY | STEROID-RECEPTOR | RIBULOSE-BISPHOSPHATE CARBOXYLASE | HISTONE CHAPERONES | HEAT-SHOCK-PROTEIN | Stress, Physiological - physiology | Adaptation, Physiological - physiology | Molecular Chaperones - physiology | Humans | Neoplasms | Care and treatment | Research | Molecular chaperones | Stress (Psychology) | Analysis | Cancer | Proteins | Stresses | Drug delivery | Chaperones
HSP90 INHIBITORS | ONCOLOGY | MOLECULAR CHAPERONES | PLANT-SPECIFIC THIOREDOXIN | POSTTRANSLATIONAL MODIFICATIONS | CONFORMATIONAL DYNAMICS | ANTITUMOR-ACTIVITY | STEROID-RECEPTOR | RIBULOSE-BISPHOSPHATE CARBOXYLASE | HISTONE CHAPERONES | HEAT-SHOCK-PROTEIN | Stress, Physiological - physiology | Adaptation, Physiological - physiology | Molecular Chaperones - physiology | Humans | Neoplasms | Care and treatment | Research | Molecular chaperones | Stress (Psychology) | Analysis | Cancer | Proteins | Stresses | Drug delivery | Chaperones
Journal Article
Cancer Letters, ISSN 0304-3835, 2012, Volume 323, Issue 1, pp. 29 - 40
Abstract Pancreatic tumors are resistant to conventional chemotherapies. The present study was aimed at evaluating the potential of a novel plant-derived...
Hematology, Oncology and Palliative Medicine | Natural product | Therapy | Cancer metabolism | Pancreatic cancer | APOPTOSIS | GROWTH-INHIBITION | HYPOXIA | ANTITUMOR | GEMCITABINE | NECROSIS | ONCOLOGY | ANNONA-MURICATA | MUC4 MUCIN | EXPRESSION | ACETOGENINS | Pancreatic Neoplasms - metabolism | Plant Extracts - pharmacology | Humans | Blotting, Western | Necrosis | Neoplasms, Experimental - pathology | Xenograft Model Antitumor Assays | Cell Movement - drug effects | Microscopy, Confocal | Animals | Signal Transduction - drug effects | Mice, Nude | Annona - chemistry | Cell Line, Tumor | Female | Antineoplastic Agents - pharmacology | Mice | Neoplasms, Experimental - metabolism | Phytotherapy - methods | Neoplasms, Experimental - drug therapy | Real-Time Polymerase Chain Reaction | Glucose metabolism | Chemotherapy | Care and treatment | Oncology, Experimental | Physiological aspects | Metastasis | Research | Gene expression | Cells | Tumors | Cancer | Cell culture | Surgical implants | Disease | Toxicity | Clinical trials | Cytotoxicity | Cancer therapies | Protein turnover | Metastases | Cell cycle | Biocompatibility | Inhibition | Drug dosages | NF-κB protein | Cell survival | Pharmacology | Breast cancer | Tumorigenicity | Plants | Metabolism | Chemical compounds | Biological activity | Studies | Properties (attributes) | Natural products | Medical prognosis | Glycolysis | Pheochromocytoma cells | Hypoxia | Diabetes | cancer metabolism | therapy | natural product
Hematology, Oncology and Palliative Medicine | Natural product | Therapy | Cancer metabolism | Pancreatic cancer | APOPTOSIS | GROWTH-INHIBITION | HYPOXIA | ANTITUMOR | GEMCITABINE | NECROSIS | ONCOLOGY | ANNONA-MURICATA | MUC4 MUCIN | EXPRESSION | ACETOGENINS | Pancreatic Neoplasms - metabolism | Plant Extracts - pharmacology | Humans | Blotting, Western | Necrosis | Neoplasms, Experimental - pathology | Xenograft Model Antitumor Assays | Cell Movement - drug effects | Microscopy, Confocal | Animals | Signal Transduction - drug effects | Mice, Nude | Annona - chemistry | Cell Line, Tumor | Female | Antineoplastic Agents - pharmacology | Mice | Neoplasms, Experimental - metabolism | Phytotherapy - methods | Neoplasms, Experimental - drug therapy | Real-Time Polymerase Chain Reaction | Glucose metabolism | Chemotherapy | Care and treatment | Oncology, Experimental | Physiological aspects | Metastasis | Research | Gene expression | Cells | Tumors | Cancer | Cell culture | Surgical implants | Disease | Toxicity | Clinical trials | Cytotoxicity | Cancer therapies | Protein turnover | Metastases | Cell cycle | Biocompatibility | Inhibition | Drug dosages | NF-κB protein | Cell survival | Pharmacology | Breast cancer | Tumorigenicity | Plants | Metabolism | Chemical compounds | Biological activity | Studies | Properties (attributes) | Natural products | Medical prognosis | Glycolysis | Pheochromocytoma cells | Hypoxia | Diabetes | cancer metabolism | therapy | natural product
Journal Article
Cancer Research, ISSN 0008-5472, 08/2015, Volume 75, Issue 15 Supplement, pp. 1256 - 1256
Journal Article
Clinical oncology (Royal College of Radiologists (Great Britain)), ISSN 0936-6555, 03/2011
This article has been withdrawn at the request of the author(s) and/or editor. The Publisher apologizes for any inconvenience this may cause. The full Elsevier...
Journal Article
Cancer and Metastasis Reviews, ISSN 0167-7659, 12/2015, Volume 34, Issue 4, pp. 593 - 609
Mucins are heavily O-glycosylated proteins primarily produced by glandular and ductal epithelial cells, either in membrane-tethered or secretory forms, for...
Biomedicine | Mucins | Synteny | Knockout models | Cancer Research | Oncology | Vaccines | Transgenic mice models | Biomedicine general | Cancer | CHROMOSOMAL LOCALIZATION | PANCREATIC-CANCER | TISSUE-SPECIFIC EXPRESSION | TUMOR-ASSOCIATED MUCIN | OVARIAN-CANCER | BOWEL-DISEASE | GROWTH-FACTOR RECEPTOR | ONCOLOGY | GENE-EXPRESSION | MOLECULAR-CLONING | ABERRANT EXPRESSION | Antigens, Neoplasm - genetics | Inflammation - pathology | Prognosis | Humans | Disease Progression | Mice, Knockout | Mucous Membrane - metabolism | Animals | Genetic Engineering | Mice | Neoplasms - pathology | Mucins - genetics | Disease Models, Animal | Analysis | Genetically modified organisms | Physiological aspects | Models | Genetic engineering | Inflammation
Biomedicine | Mucins | Synteny | Knockout models | Cancer Research | Oncology | Vaccines | Transgenic mice models | Biomedicine general | Cancer | CHROMOSOMAL LOCALIZATION | PANCREATIC-CANCER | TISSUE-SPECIFIC EXPRESSION | TUMOR-ASSOCIATED MUCIN | OVARIAN-CANCER | BOWEL-DISEASE | GROWTH-FACTOR RECEPTOR | ONCOLOGY | GENE-EXPRESSION | MOLECULAR-CLONING | ABERRANT EXPRESSION | Antigens, Neoplasm - genetics | Inflammation - pathology | Prognosis | Humans | Disease Progression | Mice, Knockout | Mucous Membrane - metabolism | Animals | Genetic Engineering | Mice | Neoplasms - pathology | Mucins - genetics | Disease Models, Animal | Analysis | Genetically modified organisms | Physiological aspects | Models | Genetic engineering | Inflammation
Journal Article
Breast Cancer Research and Treatment, ISSN 0167-6806, 7/2018, Volume 170, Issue 1, pp. 189 - 196
Breast and/or ovarian cancers are among the most common cancers in women across the world. In the Indian population, the healthcare burden of breast and/or...
Multi-gene panel | Next-generation sequencing | Medicine & Public Health | Oncology | Breast cancer | BRCA1 | BRCA2 | DIAGNOSIS | MANAGEMENT | SERIES | HEREDITARY BREAST | RISK | SUSCEPTIBILITY GENES | CARE | ONCOLOGY | FREQUENCY | GERMLINE MUTATIONS | Genetic Predisposition to Disease | Early Detection of Cancer | Fanconi Anemia Complementation Group N Protein - genetics | Ovarian Neoplasms - diagnosis | Humans | Middle Aged | Ovarian Neoplasms - pathology | India - epidemiology | Tumor Suppressor Protein p53 - genetics | Ovarian Neoplasms - epidemiology | Ovarian Neoplasms - genetics | BRCA1 Protein - genetics | Breast Neoplasms - genetics | Mass Screening | Breast Neoplasms - pathology | Germ-Line Mutation | Adult | Female | Aged | Breast Neoplasms - diagnosis | Breast - pathology | BRCA2 Protein - genetics | Breast Neoplasms - epidemiology | Genes | Genetic aspects | Tumor proteins | Genetic screening | Ovarian cancer | Cancer
Multi-gene panel | Next-generation sequencing | Medicine & Public Health | Oncology | Breast cancer | BRCA1 | BRCA2 | DIAGNOSIS | MANAGEMENT | SERIES | HEREDITARY BREAST | RISK | SUSCEPTIBILITY GENES | CARE | ONCOLOGY | FREQUENCY | GERMLINE MUTATIONS | Genetic Predisposition to Disease | Early Detection of Cancer | Fanconi Anemia Complementation Group N Protein - genetics | Ovarian Neoplasms - diagnosis | Humans | Middle Aged | Ovarian Neoplasms - pathology | India - epidemiology | Tumor Suppressor Protein p53 - genetics | Ovarian Neoplasms - epidemiology | Ovarian Neoplasms - genetics | BRCA1 Protein - genetics | Breast Neoplasms - genetics | Mass Screening | Breast Neoplasms - pathology | Germ-Line Mutation | Adult | Female | Aged | Breast Neoplasms - diagnosis | Breast - pathology | BRCA2 Protein - genetics | Breast Neoplasms - epidemiology | Genes | Genetic aspects | Tumor proteins | Genetic screening | Ovarian cancer | Cancer
Journal Article
Nature Communications, ISSN 2041-1723, 12/2018, Volume 9, Issue 1, pp. 4345 - 15
Environmental and genetic risk factors contribute to Parkinson's Disease (PD) pathogenesis and the associated midbrain dopamine (mDA) neuron loss. Here, we...
ONSET PARKINSONISM | PINK1 | PROTEIN | MITOCHONDRIAL | MOLECULAR CHAPERONES | INFLAMMATION | MULTIDISCIPLINARY SCIENCES | PARKINSON-DISEASE | NF-KAPPA-B | CANCER | STEM | Mesencephalon - metabolism | Dopaminergic Neurons - metabolism | HSP90 Heat-Shock Proteins - physiology | Biosensing Techniques | Stress, Physiological | HSP90 Heat-Shock Proteins - metabolism | NF-kappa B - metabolism | STAT3 Transcription Factor - metabolism | Mesencephalon - pathology | Chemical sensors | Networks | Hsp90 protein | Parkinson's disease | Mesencephalon | Change detection | Pathogenesis | Innovations | Activation | Tyrosine 3-monooxygenase | Risk factors | Signal transduction | Pathways | Sensors | Movement disorders | Stresses | Tyrosine | NF-κB protein | Dopamine | Neurodegenerative diseases | Neurons | Hydroxylase | Stat3 protein | Health risks | Pharmacology | Risk analysis | Stress | Neurological diseases | Organic chemistry | Signaling | Stem cells | Biosensors | Viability | Pluripotency | Index Medicus
ONSET PARKINSONISM | PINK1 | PROTEIN | MITOCHONDRIAL | MOLECULAR CHAPERONES | INFLAMMATION | MULTIDISCIPLINARY SCIENCES | PARKINSON-DISEASE | NF-KAPPA-B | CANCER | STEM | Mesencephalon - metabolism | Dopaminergic Neurons - metabolism | HSP90 Heat-Shock Proteins - physiology | Biosensing Techniques | Stress, Physiological | HSP90 Heat-Shock Proteins - metabolism | NF-kappa B - metabolism | STAT3 Transcription Factor - metabolism | Mesencephalon - pathology | Chemical sensors | Networks | Hsp90 protein | Parkinson's disease | Mesencephalon | Change detection | Pathogenesis | Innovations | Activation | Tyrosine 3-monooxygenase | Risk factors | Signal transduction | Pathways | Sensors | Movement disorders | Stresses | Tyrosine | NF-κB protein | Dopamine | Neurodegenerative diseases | Neurons | Hydroxylase | Stat3 protein | Health risks | Pharmacology | Risk analysis | Stress | Neurological diseases | Organic chemistry | Signaling | Stem cells | Biosensors | Viability | Pluripotency | Index Medicus
Journal Article
Oncotarget, ISSN 1949-2553, 2014, Volume 5, Issue 17, pp. 7272 - 7284
Journal Article
Molecular Oncology, ISSN 1574-7891, 08/2016, Volume 10, Issue 7, pp. 1063 - 1077
The majority of pancreatic cancer (PC) patients are clinically presented with obstructive jaundice with elevated levels of circulatory bilirubin and alkaline...
FAK | FXR | c-Jun | Bile acids | MUC4 | Pancreatic cancer | c‐Jun | ONCOLOGY | ESOPHAGUS | Pancreatic Neoplasms - blood | Transcription, Genetic - drug effects | Bile Acids and Salts - pharmacology | Focal Adhesion Protein-Tyrosine Kinases - metabolism | Mucin-4 - metabolism | Pancreatic Neoplasms - pathology | Pancreatic Neoplasms - enzymology | Mice, Transgenic | Pancreatic Neoplasms - genetics | Protein Transport - drug effects | Enzyme Activation - drug effects | Up-Regulation - drug effects | Animals | Cell Nucleus - metabolism | Signal Transduction - drug effects | Proto-Oncogene Proteins c-jun - metabolism | Base Sequence | Cell Line, Tumor | Gene Expression Regulation, Neoplastic - drug effects | Cell Nucleus - drug effects | Receptors, Cytoplasmic and Nuclear - metabolism | Medical colleges | Phosphatases | Promoters (Genetics) | Analysis | Oncology, Experimental | Mucins | Metastasis | Bilirubin | Research | Cancer | Jaundice | Cholecystectomy | Animal models | Gallbladder diseases | Kinases | Patients | Metastases | Studies | Acids | Transcription activation | Pheochromocytoma cells | Focal adhesion kinase | Bile | Tumors
FAK | FXR | c-Jun | Bile acids | MUC4 | Pancreatic cancer | c‐Jun | ONCOLOGY | ESOPHAGUS | Pancreatic Neoplasms - blood | Transcription, Genetic - drug effects | Bile Acids and Salts - pharmacology | Focal Adhesion Protein-Tyrosine Kinases - metabolism | Mucin-4 - metabolism | Pancreatic Neoplasms - pathology | Pancreatic Neoplasms - enzymology | Mice, Transgenic | Pancreatic Neoplasms - genetics | Protein Transport - drug effects | Enzyme Activation - drug effects | Up-Regulation - drug effects | Animals | Cell Nucleus - metabolism | Signal Transduction - drug effects | Proto-Oncogene Proteins c-jun - metabolism | Base Sequence | Cell Line, Tumor | Gene Expression Regulation, Neoplastic - drug effects | Cell Nucleus - drug effects | Receptors, Cytoplasmic and Nuclear - metabolism | Medical colleges | Phosphatases | Promoters (Genetics) | Analysis | Oncology, Experimental | Mucins | Metastasis | Bilirubin | Research | Cancer | Jaundice | Cholecystectomy | Animal models | Gallbladder diseases | Kinases | Patients | Metastases | Studies | Acids | Transcription activation | Pheochromocytoma cells | Focal adhesion kinase | Bile | Tumors
Journal Article
Composites Part A, ISSN 1359-835X, 03/2019, Volume 118, pp. 150 - 161
In the past, various analytical and semi-analytical permeability models have been implemented for process modeling of flow through single scale fabric with...
Filament distribution | SEM | Liquid composite molding | Transverse tow permeability | RESIN | REINFORCEMENTS | WOVEN FIBER PREFORMS | UNSATURATED FLOW | LIQUID | COMPRESSIBILITY | MATERIALS SCIENCE, COMPOSITES | RTM | FLOW PERMEABILITY | ENGINEERING, MANUFACTURING | IMPREGNATION | Textile fabrics | Models | Permeability | Mechanical engineering | Analysis | Aerospace engineering
Filament distribution | SEM | Liquid composite molding | Transverse tow permeability | RESIN | REINFORCEMENTS | WOVEN FIBER PREFORMS | UNSATURATED FLOW | LIQUID | COMPRESSIBILITY | MATERIALS SCIENCE, COMPOSITES | RTM | FLOW PERMEABILITY | ENGINEERING, MANUFACTURING | IMPREGNATION | Textile fabrics | Models | Permeability | Mechanical engineering | Analysis | Aerospace engineering
Journal Article
American Journal of Physiology - Gastrointestinal and Liver Physiology, ISSN 0193-1857, 02/2011, Volume 300, Issue 2, pp. 264 - 272
Epithelial proliferation, critical for homeostasis, healing, and colon cancer progression, is in part controlled by epidermal growth factor receptor (EGFR)....
FOXO3 | EGFR | Colon | PHYSIOLOGY | GROWTH-FACTOR-RECEPTOR | CANCER CELLS | PHOSPHATIDYLINOSITOL 3-KINASE | DOWN-REGULATION | CYCLE ARREST | BETA-CATENIN | INTESTINAL EPITHELIAL-CELLS | P27(KIP1) | FORKHEAD TRANSCRIPTION FACTORS | IN-VITRO | colon | GASTROENTEROLOGY & HEPATOLOGY | Intestinal Mucosa - metabolism | Phosphorylation | Cell Proliferation | Signal Transduction | Colon - pathology | Down-Regulation | Humans | Phosphatidylinositol 3-Kinases - metabolism | Colon - metabolism | Colonic Neoplasms - metabolism | Mice, Knockout | Cyclin-Dependent Kinase Inhibitor p27 - metabolism | Receptor, Epidermal Growth Factor - metabolism | Animals | Cell Cycle | Forkhead Transcription Factors - metabolism | Colonic Neoplasms - pathology | Cell Line, Tumor | Cytosol - metabolism | Mice | Forkhead Box Protein O3 | Proto-Oncogene Proteins c-akt - metabolism | Forkhead Transcription Factors - deficiency | Physiological aspects | Development and progression | Care and treatment | Colon cancer | Epidermal growth factor | Mucosal Biology
FOXO3 | EGFR | Colon | PHYSIOLOGY | GROWTH-FACTOR-RECEPTOR | CANCER CELLS | PHOSPHATIDYLINOSITOL 3-KINASE | DOWN-REGULATION | CYCLE ARREST | BETA-CATENIN | INTESTINAL EPITHELIAL-CELLS | P27(KIP1) | FORKHEAD TRANSCRIPTION FACTORS | IN-VITRO | colon | GASTROENTEROLOGY & HEPATOLOGY | Intestinal Mucosa - metabolism | Phosphorylation | Cell Proliferation | Signal Transduction | Colon - pathology | Down-Regulation | Humans | Phosphatidylinositol 3-Kinases - metabolism | Colon - metabolism | Colonic Neoplasms - metabolism | Mice, Knockout | Cyclin-Dependent Kinase Inhibitor p27 - metabolism | Receptor, Epidermal Growth Factor - metabolism | Animals | Cell Cycle | Forkhead Transcription Factors - metabolism | Colonic Neoplasms - pathology | Cell Line, Tumor | Cytosol - metabolism | Mice | Forkhead Box Protein O3 | Proto-Oncogene Proteins c-akt - metabolism | Forkhead Transcription Factors - deficiency | Physiological aspects | Development and progression | Care and treatment | Colon cancer | Epidermal growth factor | Mucosal Biology
Journal Article
Carcinogenesis, ISSN 0143-3334, 07/2017, Volume 38, Issue 7, pp. 671 - 679
Alternative gene splicing, occurring ubiquitously in multicellular organisms can produce several protein isoforms with putatively different functions. The...
BREAST-CANCER | PREFERENTIAL EXPRESSION | EXTRACELLULAR-DOMAIN | PROTEIN | MUC1 SPLICE VARIANTS | ONCOLOGY | GENOMIC ORGANIZATION | EPIDERMAL-GROWTH-FACTOR | OVARIAN-CANCER | DRY EYE PATIENTS | PANCREATIC-CANCER CELLS | Multigene Family - genetics | Inflammation - pathology | Cell Proliferation - genetics | Alternative Splicing - genetics | Humans | Gene Expression Regulation, Neoplastic | Exons - genetics | Cell Movement - genetics | Mucins - biosynthesis | Neoplasms - genetics | Neoplasm Invasiveness - pathology | Inflammation - genetics | Neoplasm Invasiveness - genetics | Neoplasms - pathology | Mucins - genetics | Protein Isoforms - genetics | Index Medicus | Reviews
BREAST-CANCER | PREFERENTIAL EXPRESSION | EXTRACELLULAR-DOMAIN | PROTEIN | MUC1 SPLICE VARIANTS | ONCOLOGY | GENOMIC ORGANIZATION | EPIDERMAL-GROWTH-FACTOR | OVARIAN-CANCER | DRY EYE PATIENTS | PANCREATIC-CANCER CELLS | Multigene Family - genetics | Inflammation - pathology | Cell Proliferation - genetics | Alternative Splicing - genetics | Humans | Gene Expression Regulation, Neoplastic | Exons - genetics | Cell Movement - genetics | Mucins - biosynthesis | Neoplasms - genetics | Neoplasm Invasiveness - pathology | Inflammation - genetics | Neoplasm Invasiveness - genetics | Neoplasms - pathology | Mucins - genetics | Protein Isoforms - genetics | Index Medicus | Reviews
Journal Article
Cold Spring Harbor perspectives in biology, 04/2019
Cancer is often associated with alterations in the chaperome, a collection of chaperones, cochaperones, and other cofactors. Changes in the expression levels...
Journal Article
Oncotarget, ISSN 1949-2553, 2015, Volume 6, Issue 25, pp. 21085 - 21099
Several studies have demonstrated that MUC4 is involved in progression and metastasis of pancreatic cancer (PC). Here, we report that HER3/MUC4 interaction in...
HER2 | KPC model | MUC4 | Pancreatic cancer | HER3 | Neoplasm Transplantation | Phosphorylation | Receptor, ErbB-3 - metabolism | Cell Proliferation | Pancreatic Neoplasms - metabolism | Humans | Gene Expression Regulation, Neoplastic | Receptor, ErbB-2 - metabolism | Molecular Sequence Data | Phosphatidylinositol 3-Kinases - metabolism | Carcinogenesis | Neoplasm Metastasis | Female | Amino Acid Sequence | Signal Transduction | Mucin-4 - metabolism | Pancreatic Neoplasms - pathology | Proto-Oncogene Proteins c-myc - metabolism | Disease Progression | Sequence Homology, Amino Acid | Phenotype | Animals | Cell Cycle | Mice, Nude | Mice
HER2 | KPC model | MUC4 | Pancreatic cancer | HER3 | Neoplasm Transplantation | Phosphorylation | Receptor, ErbB-3 - metabolism | Cell Proliferation | Pancreatic Neoplasms - metabolism | Humans | Gene Expression Regulation, Neoplastic | Receptor, ErbB-2 - metabolism | Molecular Sequence Data | Phosphatidylinositol 3-Kinases - metabolism | Carcinogenesis | Neoplasm Metastasis | Female | Amino Acid Sequence | Signal Transduction | Mucin-4 - metabolism | Pancreatic Neoplasms - pathology | Proto-Oncogene Proteins c-myc - metabolism | Disease Progression | Sequence Homology, Amino Acid | Phenotype | Animals | Cell Cycle | Mice, Nude | Mice
Journal Article